NDC 45043-876

Chenodal

Chenodiol

Chenodal is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Manchester Pharmaceuticals Inc.. The primary component is Chenodiol.

• Product ID: 45043-876_d6369783-3cd7-4d99-8ddd-07102a5512f9
• NDC: 45043-876
• Product Type: Human Prescription Drug
• Proprietary Name: Chenodal
• Generic Name: Chenodiol
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2009-10-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA091019
• Labeler Name: Manchester Pharmaceuticals Inc.
• Substance Name: CHENODIOL
• Active Ingredient Strength: 250 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 45043-876-40

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (45043-876-40)

• Marketing Start Date: 2009-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 45043-876-40 [45043087640]

Chenodal TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA091019
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-10-01
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
CHENODIOL	250 mg/1

OpenFDA Data

• SPL SET ID: b8b4539b-31d1-40cb-b284-86cf8b16522a
• Manufacturer:
  • Manchester Pharmaceuticals Inc.
• UNII:
  • 0GEI24LG0J
• RxNorm Concept Unique ID - RxCUI:
  • 877417
  • 618469
• UPC Code:
  • 0345043876404

NDC Crossover Matching brand name "Chenodal" or generic name "Chenodiol"

NDC	Brand Name	Generic Name
45043-876	Chenodal	Chenodiol
68974-876	Chenodal	Chenodiol
0722-7121	Chenodiol	Chenodiol
79739-7121	Chenodiol	Chenodiol